Xu Yunzhao, Wang Chenyi, Zhang Yuquan, Jia Lizhou, Huang Jianfei
Department of Obstetrics and Gynecology, Nantong University Affiliated Hospital, Nantong 226001, Jiangsu, China.
Department of Obstetrics and Gynecology, The Affiliated People's Hospital of Inner Mongolia Medical College, Inner Mongolia Autonomous Region 010021, China.
Sci Rep. 2015 Jul 15;5:12104. doi: 10.1038/srep12104.
The cancer testis antigen, melanoma-associated antigen A9 (MAGE-A9), is expressed in many kinds of different human cancers, and is an important target for immunotherapy. However, the clinicopathologic significance of MAGE-A9 in epithelial ovarian cancer (EOC) is unknown. In this study, real-time PCR (12 carcinomas of high FIGO stage, 12 carcinomas of low FIGO stage, and 20 normal ovary or fallopian tube tissues) and immunohistochemistry by tissue microarrays (128 carcinomas and 112 normal ovary or fallopian tube tissues, benign or borderline ovarian tumor tissues) were performed to characterize expression of MAGE-A9 in EOC. We found that significantly higher MAGE-A9 mRNA expression in EOC tumors than that in normal ovary or fallopian tube tissues (all P < 0.05). Protein expression of MAGE-A9 was significantly associated with FIGO stage, high histological grade, level of CA-125 and metastasis. Consistent with the associated poor clinicopathologic features, patients with MAGE-A9(H (high-expressing)) tumors had a worse overall survival as compared to patients with MAGE-A9(L (low or none-expressing)) tumors. Further studies revealed that MAGE-A9 overexpression was an independent prognostic factor for overall survival (OS). Multivariate analysis showed that patients with MAGE-A9 overexpressing tumors had extremely poor OS. These findings indicate that MAGE-A9 expression may be helpful in predicting EOC prognosis.
癌睾丸抗原黑素瘤相关抗原A9(MAGE - A9)在多种不同的人类癌症中均有表达,是免疫治疗的重要靶点。然而,MAGE - A9在上皮性卵巢癌(EOC)中的临床病理意义尚不清楚。在本研究中,采用实时定量聚合酶链反应(对12例高国际妇产科联盟(FIGO)分期的癌、12例低FIGO分期的癌以及20例正常卵巢或输卵管组织进行检测)以及组织芯片免疫组化法(对128例癌、112例正常卵巢或输卵管组织、良性或交界性卵巢肿瘤组织进行检测)来分析EOC中MAGE - A9的表达特征。我们发现,EOC肿瘤中MAGE - A9 mRNA表达显著高于正常卵巢或输卵管组织(所有P < 0.05)。MAGE - A9的蛋白表达与FIGO分期、高组织学分级、CA - 125水平及转移显著相关。与这些不良临床病理特征一致,MAGE - A9高表达(H)肿瘤患者的总生存期较MAGE - A9低表达或无表达(L)肿瘤患者更差。进一步研究表明,MAGE - A9过表达是总生存期(OS)的独立预后因素。多因素分析显示,MAGE - A9过表达肿瘤患者的OS极差。这些发现表明,MAGE - A9表达可能有助于预测EOC预后。